chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152796907827969079CT24GENIChomozygous142486792
152796911327969114GC21GENIChomozygous142486793
152796912027969121AC21GENIChomozygous142486794
152796972527969726GA19GENIChomozygous142486795
152796985627969857CT19GENIChomozygous142486796
152797017227970173GA24GENIChomozygous142486797
152797030027970301GA28GENIChomozygous142486798
152797134427971345GT27GENIChomozygous142486799
152797136927971369AGAC22GENIChomozygous142460085
152797153127971532TC39GENIChomozygous142486800
152797171027971711G24GENIChomozygous142460086
152797214027972141GT18GENIChomozygous142486801
152797220427972205TC21GENIChomozygous142486802
152797230127972301A17GENIChomozygous142460087
152797270527972706TG21GENIChomozygous142486803
152797296227972963TC34GENIChomozygous142486804
152797410827974109AG30GENIChomozygous142486805
152797414127974142GA31GENIChomozygous142486806
152797421827974219CA25GENIChomozygous142486807
152797728427977284AGAA19GENIChomozygous142460088
152797763227977633CT25GENIChomozygous142486808